CAS 19883-75-1
:L-2-Nitrophe
Description:
L-2-Nitrophe, identified by its CAS number 19883-75-1, is a chemical compound that belongs to the class of nitrophenols. It typically features a nitro group (-NO2) attached to a phenolic structure, which can influence its reactivity and properties. This compound is characterized by its potential applications in various fields, including organic synthesis and as an intermediate in the production of dyes and pharmaceuticals. L-2-Nitrophe may exhibit moderate to high solubility in organic solvents, while its solubility in water can vary depending on the specific conditions. The presence of the nitro group can impart acidic properties, making it a weak acid. Additionally, nitrophenols are known for their potential environmental impact and toxicity, necessitating careful handling and disposal. As with many chemical substances, safety data sheets (SDS) should be consulted for information on hazards, handling precautions, and first aid measures associated with L-2-Nitrophe.
Formula:C9H10N2O4
InChI:InChI=1/C9H10N2O4/c10-7(9(12)13)5-6-3-1-2-4-8(6)11(14)15/h1-4,7H,5,10H2,(H,12,13)/t7-/m0/s1
SMILES:c1ccc(c(c1)C[C@@H](C(=O)O)N)N(=O)=O
Synonyms:- L-2-Nitrophenylalanine
- 2-Nitrophenylalanine
- 2-nitro-L-phenylalanine
- D-His(Trt)
- (2S)-2-amino-3-(2-nitrophenyl)propanoic acid
- H-PHE(2-NO2)-OH
- -2-NitrophenyL
- H-O-NITRO-PHE-OH
- L-2-AMINO-3-(2-NITRO PHENYL)-PROPIONIC ACID
- L-2-NO2-Phe-OH 2-Nitro-L-Phenylalanine
- L-2-NITROPHE
- L-PHE(2-NO2)
- L-Phenylalanine, 2-nitro-
- (S)-2-AMino-3-(2-nitrophenyl)propanoic acid
- See more synonyms
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Found 6 products.
L-Phenylalanine, 2-nitro-
CAS:Formula:C9H10N2O4Purity:97%Color and Shape:SolidMolecular weight:210.18672-Nitro-L-phenylalanine
CAS:<p>2-Nitro-L-phenylalanine</p>Formula:C9H10N2O4Purity:95%Color and Shape: white solidMolecular weight:210.19g/mol(S)-2-Amino-3-(2-nitrophenyl)propanoic acid
CAS:Formula:C9H10N2O4Purity:95%Color and Shape:SolidMolecular weight:210.1892-Nitro-L-phenylalanine
CAS:<p>2-Nitro-L-phenylalanine is an hydroxamic acid that is used in clinical photodynamic therapy for the treatment of cancer. It reacts with light to produce reactive oxygen species, which cause DNA damage and cell death. 2NPA can be found in micelles and is able to bind to quaternary ammonium salts. This active form can be produced by genetically engineered enzymes with chemical biology tools. The cleavage products are not yet fully understood, but they may include a cyclic peptide that has been shown to have antioxidant properties.</p>Formula:C9H10N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:210.19 g/molL-2-Nitrophenylalanine
CAS:Controlled Product<p>Applications L-2-Nitrophenylalanine is a derivative of L-phenylalanine (P319415), and is used in the photocleavage of polypeptide backbones. L-Phenylalanine is an essential amino acid. L-Phenylalanine is biologically converted into L-tyrosine, another one of the DNA-encoded amino acids, which in turn is converted to L-DOPA and further converted into dopamine, norepinephrine, and epinephrine.<br>References Peters, F. et al.: Chem. Biol., 16, 148 (2009); Hollunger, G. et al.: Acta Pharmacol. Toxicol., 34, 391 (1974); Bagchi, S.P. et al.: Biochem. Pharmacol., 26, 900 (1977);<br></p>Formula:C9H10N2O4Color and Shape:NeatMolecular weight:210.19





